Overview of the Analytical Method Development for Ertugliflozin Using UV and HPLC Techniques

Authors

  • Priyanka Kedar PG Scholar, PRES’s College of Pharmacy (For Women), Chincholi, Tal. Sinnar, Dist. Nashik.
  • Dr.Vinayak Gaware Associate Professor, PRES’s College of Pharmacy (For Women), Chincholi, Tal. Sinnar, Dist. Nashik.

DOI:

https://doi.org/10.22270/ajprd.v13i3.1577

Abstract

Ertugliflozin is a new sodium-glucose cotransporter 2 (SGLT2) inhibitor used to treat type 2 diabetes. Because of its extensive use, it is critical to develop precise and reliable analytical methods for determining its presence in pharmaceutical formulations and biological materials. Several analytical methods have been developed to determine ertugliflozin, including UV spectroscopy, HPLC, and LC-MS/MS. Ertugliflozin has been measured using UV spectroscopy in pharmaceutical formulations and HPLC in biological samples. LC-MS/MS has been used for the determination of ertugliflozin in biological samples, providing high sensitivity and specificity. The analytical method development for ertugliflozin involves several steps, including method validation, optimization of chromatographic conditions, and selection of suitable detectors. Method validation involves evaluating the accuracy, precision, specificity, and robustness of the analytical method. Optimization of chromatographic conditions involves selecting suitable columns, mobile phases, and detection wavelengths. Selection of suitable detectors involves choosing detectors that provide high sensitivity and specificity. This review provides an overview of the analytical method development for ertugliflozin using UV and HPLC techniques. The review highlights the importance of method validation, optimization of chromatographic conditions, and selection of suitable detectors in analytical method development. UV and HPLC techniques have been widely used for the determination of ertugliflozin, providing high sensitivity and specificity. This review provides an overview of the analytical method development for ertugliflozin using UV and HPLC techniques, highlighting the importance of method validation, optimization of chromatographic conditions, and selection of suitable detectors.

 

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Author Biographies

Priyanka Kedar, PG Scholar, PRES’s College of Pharmacy (For Women), Chincholi, Tal. Sinnar, Dist. Nashik.

PG Scholar, PRES’s College of Pharmacy (For Women), Chincholi, Tal. Sinnar, Dist. Nashik.

Dr.Vinayak Gaware, Associate Professor, PRES’s College of Pharmacy (For Women), Chincholi, Tal. Sinnar, Dist. Nashik.

Associate Professor, PRES’s College of Pharmacy (For Women), Chincholi, Tal. Sinnar, Dist. Nashik.

References

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Singh R, et al. Development and validation of a UV spectrophotometric method for the determination of ertugliflozin in human plasma. J Pharm Pharmacol. 2020;72(8):1086–1095.

Gupta S, et al. Simultaneous determination of ertugliflozin and its metabolites in human urine using HPLC-MS/MS. J Chromatogr B. 2020;1139:121965.

Kumar P, et al. Development and validation of a reversed-phase HPLC method for the determination of ertugliflozin in bulk and pharmaceutical formulations. J LiqChromatogrRelat Technol. 2020;43(1):1–8.

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Kumar P, et al. Recent advances in the analytical methods for the determination of ertugliflozin. J Chromatogr B. 2020;1139:121965.

Kumar P, et al. Development and validation of a reversed-phase HPLC method for the determination of ertugliflozin in bulk and pharmaceutical formulations. ProcIntConf Anal Chem. 2020:123–126.

Singh R, et al. Development and validation of a UV spectrophotometric method for the determination of ertugliflozin in human plasma. ProcIntConf Pharm Pharmacol. 2020:156–159.

Published

2025-06-15

How to Cite

Priyanka Kedar, & Dr.Vinayak Gaware. (2025). Overview of the Analytical Method Development for Ertugliflozin Using UV and HPLC Techniques. Asian Journal of Pharmaceutical Research and Development, 13(3), 162–166. https://doi.org/10.22270/ajprd.v13i3.1577